Group El Eulj
⚠️ Moderate Risk
FEI: 3010291397 • Casablanca, Casablanca • MOROCCO
FEI Number
3010291397
Location
Casablanca, Casablanca
Country
MOROCCOAddress
Km 10 5 Route El Jadida, , Casablanca, Casablanca, Morocco
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
FLAVR LBLG
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an artificial flavoring and it fails to bear labeling stating that fact.
JUICE %
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that the food purports to be a beverage containing vegetable or fruit juice and does not bear a statement on the label in appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained therein.
USUAL NAME
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/24/2013 | 20KDT06ORANGE, CITRUS FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 9/24/2013 | 21DDT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 9/24/2013 | 29BHT50SOFT DRINK, COLA, CARBONATED | New York District Office (NYK-DO) | |
| 9/24/2013 | 21VDT07PINEAPPLE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Group El Eulj's FDA import refusal history?
Group El Eulj (FEI: 3010291397) has 4 FDA import refusal record(s) in our database, spanning from 9/24/2013 to 9/24/2013.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Group El Eulj's FEI number is 3010291397.
What types of violations has Group El Eulj received?
Group El Eulj has been cited for 9 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Group El Eulj come from?
All FDA import refusal data for Group El Eulj is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.